| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21599766-21600179 | Common:1; Rare:133 | ||||
| chr16:21600269-21600300 | Rare:9 | ||||
| chr16:21952432-21952649 | Rare:37 | ||||
| chr16:21952856-21953413 | Common:1; Rare:132; Clinvar (benign):3 | ||||
| chr16:22007596-22007804 | Common:2; Rare:58 | ||||
| chr16:22007987-22008180 | Rare:63 | ||||
| chr16:22205766-22205949 | Rare:25 | ||||
| chr16:22205984-22206374 | Common:1; Rare:101 | ||||
| chr16:22296860-22297142 | Common:4; Rare:93 | ||||
| chr16:22297150-22297485 | Common:3; Rare:172 | ||||
| chr16:22297655-22297764 | Common:1; Rare:22 | ||||
| chr16:22297789-22297946 | Common:1; Rare:39 | ||||
| chr16:22374345-22374404 | Rare:14 | ||||
| chr16:22374479-22374928 | Common:1; Rare:154 | ||||
| chr16:22375047-22375122 | Common:2; Rare:18 |